Muriatic Acid and 3% Hydrogen Peroxide First Attempt
2014-04-10 by <kbyrne10@...>
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2014-04-10 by <kbyrne10@...>
2014-04-10 by <leeleduc@...>
2014-04-10 by <beefyzee@...>
2014-04-10 by <kbyrne10@...>
2014-04-11 by <kbyrne10@...>
2014-04-11 by Harvey White
On 10 Apr 2014 11:09:00 -0700, you wrote: >I just tried another version of etchant solution. 1. Lowels lumber yard Crown Muriatic Acid and 2. Drug store version of hydrogen peroxide 3 % type. Mix 1 & 1/2 cup muriatic acid and 3/4 cup hydrogen peroxide in a plastic tupper ware container. My board size was equal to 4 in. times 8 in. Time > around. 30 min. My question is I do not know the strength of the Crown version > of the muriatic acid. Is this time normal and is there a way to speed up the time the board is in the tray I think less muriatic acid and more H2O2, say 1 part to 4 parts or 1 part to 3 parts. Harvey
2014-04-11 by Mike Law
Just to chip in my 2 cents: 25% HCl (in the UK, maybe ask for "spirits of salt" at the hardware type shop). 3% peroxide from the chemist. First etch - nice and quick. All further etches, not worth bothering with - think overnight! So I went on Ebay and got the food grade 35% H2O2 peroxide. Outside, raining, temp not much above 10*C (I was in the garage, so it wasn't raining on my PCB!). Threw in H2O2 until it went the lovely emerald green colour. Chucked in the board, got a stick to swish stuff around, and yeah - like Dexter's Lab - bubbles, smoking, all very exciting. For those with bubble tanks, etching many boards, I'd pay attention to specific gravity and all the fancy sciency bits. For people like me who want a board every once in a while: get the acid, throw in some stupidly strong peroxide and swish it about a bit until it "looks right". Obviously it doesn't go green until you've got some copper in there, so don't go made to begin with. I like the foam brush idea, I'll try that (or a sponge) next time. But don't faff about with 3% peroxide in my opinion, just throw in something stronger and have fun with the bubbling and smoking! J Mike As an aside, HCl for cleaning stubborn stains from lavatory pans is excellent. Throw it on, leave for 20 mins, rinse off. Sparkling loo, zero effort!
From: Homebrew_PCBs@yahoogroups.com [mailto:Homebrew_PCBs@yahoogroups.com] On Behalf Of Harvey White Sent: 11 April 2014 03:21 To: Homebrew_PCBs@yahoogroups.com Subject: [Bulk] Re: [Homebrew_PCBs] Muriatic Acid and 3% Hydrogen Peroxide First Attempt On 10 Apr 2014 11:09:00 -0700, you wrote: >I just tried another version of etchant solution. 1. Lowels lumber yard Crown Muriatic Acid and 2. Drug store version of hydrogen peroxide 3 % type. Mix 1 & 1/2 cup muriatic acid and 3/4 cup hydrogen peroxide in a plastic tupper ware container. My board size was equal to 4 in. times 8 in. Time > around. 30 min. My question is I do not know the strength of the Crown version > of the muriatic acid. Is this time normal and is there a way to speed up the time the board is in the tray I think less muriatic acid and more H2O2, say 1 part to 4 parts or 1 part to 3 parts. Harvey [Non-text portions of this message have been removed]
2014-04-14 by <soffee83@...>
2014-04-14 by Harvey White
On 14 Apr 2014 12:10:34 -0700, you wrote: >"H2O2 can degrade with temperature and time." > >- I wondered about that shelf life thing, but didn't know if my acid was the one that had gone bad. The past few etches have turned out OK, but seemed to take forever. When I first got attached to that method I was really impressed by how fast it worked and how forgiving it was about conditions and agitation. I remember etching outside in the late fall or winter (I think it was even rainy) and it would burn away so fast that I had to rip it out of the solution after a couple minutes or it would eat through the thinner traces. That's too fast, you don't get enough control. The reaction is essentially an oxidization of copper, so the more oxygen (and warmer the solution) the faster. The normal way is to add oxygen by bubbling, your option on using the H2O2, but you don't want to dilute the solution. The normal etch time on a board has been mentioned to be about 12 minutes. > >I need to get that going again. I'll probably start with all new chemicals and if that doesn't do it, I'll track down the stronger H2O2 you guys are talking about. All new chemicals will etch faster because of the increased oxygen. That's why the brushing of the board with a brush works, (as long as the resist stays on the board, that is). Agitation keeps a fresh flow of etchant to the board, one reason why spray etching works well, as long as it is even. Harvey > >George
2014-04-15 by <soffee83@...>
2014-04-15 by Harvey White
On 15 Apr 2014 08:29:03 -0700, you wrote: >Thanks Harvey, > >That time estimate was a slight exaggeration, but it probably wasn't a lot more (maybe 5min or so tops). I've had etch times in the 5 to 6 minutes range, but that was bubbling fresh H2O2 and heating the solution during the summer. No wonder. Never was quite so fast. >I'm also usually doing smaller sized boards. Re: the agitation and heat - That was one of the things I really liked when it was working well at first. It seemed to heat itself up, even in cold weather, and bubble and fizz enough where at the most, I might have stirred the top layer around a bit with a plastic knife, but on the small stuff it barely even needed that. This is an exothermic reaction, producing heat. That it bubbles and fizzes so much says that the reaction is likely going way too fast. Problem with that is there is a bit of slop time (to a point) the slower the reaction goes, you'll always undercut to some extent. Obviously a problem with finer traces, not a problem with 0.1 inch traces for power supplies. The evenness of the etch is more important that the etch time, so if you do bubble etch, you want a good (and uniform) bubble curtain. > >I built a flat vertical plexiglass tank years back, complete with a bubbler and heater, but that was when I was doing ferric chloride (and later, sodium persulfate). It was messy and hard to clean, and I was thankful that the new etchant didn't need all that, but I may start using the bubbler with it and just dropping the tube in by hand. It doesn't absolutely need it, but once it changes to CuCl, then it will. No oxygen left for the reaction. I'd like to do sodium persulfate, but I have no good (inexpensive read.....) source for it. Had done Ferric Chloride, and never again, thanks. Harvey
> >Thanks for all the tips on the stuff, > >George